Biologically active amides

ABSTRACT

Peptides, acid addition salts, salts, and pharmaceutical compositions thereof, and their use as morphine agonists, and especially Tyr.D.Met.Gly.Phe(4NO 2 ).ProNH 2  and Tyr.D-Met(O).Gly.Phe(4NO 2 ).ProNH 2  as anti-diarrhoeals and anti-tussives.

This is a division of application Ser. No. 927,271, filed July 24, 1978,now U.S. Pat. No. 4,244,944.

This invention relates to peptides and derivatives thereof; to thepreparation of such compounds; to formulations containing such compoundsand the preparation of such formulations; and to the use of thecompounds in human and veterinary medicine.

More particularly the present invention relates to peptides andderivatives thereof which exhibit morphine agonist activity. Asgenerally accepted and as the term is used herein, a morphine agonist isa compound the biological activity of which mimics that of the naturalalkaloid.

The pharmacological properties and therapeutic uses of morphine are welldocumented in the literature, see for example "The Pharmacological Basisof Therapeutics", Goodman, L. S. and Gilman, A. eds., published by TheMacMillan Company, New York, third edition (1965) especially at Chapter15, pages 247 to 266, and "Martindale: The Extra Pharmacopoeia", Blacow,N. W. ed., published by The Pharmaceutical Press, London, twenty-sixthedition (1972) especially at pages 1100 to 1106, all of which isincorporated herein by reference hereto. As is well known however(Goodman, L. S. et al., loc. cit, Chapter 16) repeated administration ofmorphine can lead to the recipient developing an addiction to the drugand tolerance to its effects and to his manifesting withdrawal symptomswhen administration is discontinued. For many years therefore researchhas been conducted with the aim of obtaining a compound having theactivity spectrum of morphine while lacking its disadvantages.

The present invention provides the novel peptides of formula (I):##STR1## together with their salts and acid addition salts, whichcompounds exhibit morphine agonist activity in both in vitro and in vivotests.

In formula (I):

R¹ is hydrogen or alkyl;

X¹ and X² are the same or different and each is the radical of a basicamino acid (D or L);

X³ is an L-radical of formula ##STR2## where Q¹ is selected fromhydroxy, alkoxy, alkanoyloxy, alkyl, nitro, trifluoromethyl, amino,N-alkylamino, N,N-dialkylamino, halogen and benzyloxy and R³ is hydrogenor alkyl;

X⁴ is a D-radical of formula ##STR3## where the Alkyl has 1 to 3 carbonatoms, Z is selected from --O--, --S--, --SO-- and --SO₂ --, a is 1, 2or 3 and b is 0 or 1;

X⁶ is an L-radical of formula ##STR4## where Q² is selected fromhydroxy, alkoxy, alkanoyloxy, alkyl, nitro, trifluoromethyl, amino,N-alkylamino, N,N-dialkylamino, halogen, benzyloxy, methyl sulphide,methyl sulphoxide, methylsulphone and hydrogen and R⁴ is hydrogen oralkyl;

X⁷ is selected from L-prolyl, L-hydroxyprolyl, L-homoprolyl,L-pipecolinyl, L-threonyl, L-seryl, cycloleucyl, D-prolyl,D-hydroxyprolyl, D-methionyl, D-methionyl sulphoxide, D-methionylsulphone, D-isoleucyl, D-norleucyl, D-valyl, D-norvalyl, D-seryl,D-threonyl, D-homoprolyl, D-pipecolinyl and D-alanyl;

X⁸ and X⁹ are the same or different and each is selected from seryl (Dor L) and threonyl (D or L);

R² is selected from a group --OR⁵, where R⁵ is hydrogen or alkyl, and agroup --NR⁶ R⁷ where R⁶ and R⁷ are the same or different and each isselected from hydrogen, alkyl and benzyl or R⁶, R⁷ and the nitrogen atomto which they are attached together comprise a group selected frompyrrolidino, piperidino and morpholino; or

R² represents a group, replacing the 1-carboxyl group of the C-terminalamino acid residue, of formula --CH₂ OR⁸ where R⁸ is hydrogen oralkanoyl; and

m, n, p and q are each selected from 0 and 1; provided that when m, n, pand q are each 0;

R¹ is hydrogen;

X³ is L-tyrosyl;

X⁴ is D-methionyl, D-methionyl sulphoxide or D-methionyl sulphone;

X⁶ is L-phenylalanyl, -4-nitrophenylalanyl, L-4-chlorophenylalanyl orL-4-methylphenylalanyl;

X⁷ is L-prolyl, D-prolyl, D-methionyl, D-methionyl sulphoxide,D-methionyl sulphone, D-leucyl or cycloleucyl;

then R² is other than a group --NR⁶ R⁷ wherein

one of R⁶ and R⁷ is hydrogen and the other is alkyl or benzyl or wherein

R⁶, R⁷ and the nitrogen atom to which they are attached togethercomprise a morpholino, piperidino or pyrrolo radical group;

furthermore that when X⁶ is L-phenylalanyl and X⁷ is L-prolyl then R³ isa group -CH₂ OR⁸ as above defined.

The abbreviations used herein for amino acids and their radicals arethose conventional in the art and may be found in, for example,Biochemistry, 11, 1726 (1972). In the above and throughout the followingall references are to the L-amino acids and their radicals except in thecase of glycine and unless otherwise stated.

By the term "basic amino acid" is herein meant an amino acid having twobasic functions and one carboxyl group, and as examples of the radicalsX¹ and X² may be mentioned lysyl (D and L), homoarginyl (D and L),ornithyl (D and L), histidyl (D and L), α,γ-diaminobutyryl (D and L) andarginyl (D and L).

In formula (I) the alkyl identities for Q¹, Q², R¹, R³, R⁴, R⁵, R⁶ andR⁷, the alkyl moiety or moieties of the alkoxy, alkanoyloxy,N-alkylamino and N,N-dialkylamino identities for Q¹ and Q² and the alkylmoiety of the alkanoyl identity for R⁸ desirably each have 1 to 4 carbonatoms and preferably 1 or 2 carbon atoms, i.e. methyl or ethyl. In theN,N-dialkylamino identities for Q¹ and Q² the alkyl moieties may be thesame or different. The halogen identities for Q¹ and Q² may each beselected from fluorine, chlorine, bromine and iodine.

Amongst the identities for X⁴ may particularly be mentioned thefollowing radicals: ##STR5##

together with the corresponding sulphoxides and sulphones.

In the acid addition salts of the peptides of formula (I) the activityresides in the base and the acid is of less importance although fortherapeutic purposes it is preferably pharmacologically andpharmaceutically acceptable to the recipient. Examples of such suitableacids include (a) mineral acids: hydrochloric, hydrobromic, phosphoric,metaphosphoric, nitric and sulphuric acids; (b) organic acids: tartaric,acetic, citric, malic, lactic, fumaric, benzoic, glycollic, gluconic,gulonic, succinic and arylsulphonic, for example p-toluenesulphonic,acids. The pharmaceutically and pharmacologically acceptable acidaddition salts together with those salts which are not so acceptable(for example salts of hydrofluoric and perchloric acids) have utility inisolation and purification of the bases, and of course the unacceptablesalts are also valuable in the preparation of the acceptable salts bytechniques well known in the art. Those peptides containing a pluralityof free amino groups may be obtained in the form of mono- or poly-acidaddition salts, or as mixed salts of a plurality of acids.

Likewise in the salts of the peptides (comprising the peptide as thecarboxylate anion together with a cation) the identity of the cation isof less importance although for therapeutic purposes it is preferablypharmacologically and pharmaceutically acceptable to the recipient.Examples of such suitable cations include sodium and potassium.

The morphine agonist properties of the peptides of formula (I) and theirsalts and acid addition salts include the following, which are givensolely by way of illustration and should be understood to benon-limiting.

(A) In vitro:

(i) Inhibition of neurally evoked contractions of the isolated mouse vasdeferens when tested by the method of Hughes et al (Brain Research, 88(1975) 296) (using pulses at 0.1 Hz), the inhibition being abolished bythe known narcotic antagonist naloxone (1-N-allyl-7,8-dihydro-14-hydroxynormorphinone).

(ii) Reduction of electrically-induced contractions of the isolatedguinea-pig ileum when prepared for stimulation after the manner of Paton(Brit. J. Pharmacol., 12 (1957) 119-127). (Each intestinal segment wasimpaled by the anode and suspended with a 2-3 g load. Stimulusparameters: frequency: 0.1 Hz; duration: 0.4 ms; voltage (supramaximal)30-40 V; the contractions were transduced isotonically).

(B) In vivo:

(i) The compounds exhibit analgesic activity, for example they areeffective in mice in the "hot plate" procedure standard in the art whentested by a modification of the method of Eddy, N. B. et al. (J. Pharm.Exp. Therap. 107, 385 (1953)), the compounds being administered byintracerebronventricular injection, and this activity is abolished bynaloxone.

As a further example the compounds are effective in reducing aceticacid-induced writhing in mice when tested by a modification of themethod of Henderson et. al., J. Pharm. Exp. Therap. 125 (1959), 237; thecompounds being administered orally and this reduction in writhing isabolished by naloxone.

(iii) The compounds exhibit antitussive activity, for example whentested in guinea-pigs according to the method of Boura et al. Brit. J.Pharmacol., 39, (1970) 225.

(iv) The compounds exhibit antidiarrhoeal activity, for example they areeffective in reducing castor oil-induced diarrhoea in rats.

The peptides of formula (I), their salts and acid addition salts whenassessed by a number of standard pharmacological procedures, have alsobeen found both to induce and to maintain anaesthesia in laboratoryanimals including rats and mice. The compounds are effective in thisrespect when administered by a variety of routes including parenteral,for example by intravenous or intracerebroventricular injection.Illustrative of the anaesthetic effects of the compounds are thefollowing, which should be understood to be non-limiting.

(i) Abolition of the righting reflex. This is characteristic ofrecognised anaesthetic agents such as chloral hydrate(2,2,2-trichloro-1,1-ethanediol), urethan (ethyl carbamate) and thebarbiturates (derivatives of barbituric acid). An animal lacking thisreflex does not roll over or attempt to regain its normal posture whenplaced on its back.

(ii) Abolition of the pinnal reflex. In this procedure a wire or similarprobe is introduced into the ear pinna; in the normal (control) animalthere is a resultant reflex twitch or shake of the affected pinna.

(iii) Abolition of the corneal reflex. In this procedure the cornea islightly touched with a wire or similar; in the normal (control) animalthere is a resultant reflex blink of the eyelids. This reflex is ofclinical importance in man in that it is one of the last reflexes to beabolished during the induction of general anaesthesia.

Each of the foregoing effects (i), (ii) and (iii) may be reversed byadministration of the known narcotic antagonist naloxone(1-N-allyl-7,8-dihydro-14-hydroxynormorphinone). However it has beenfound that morphine itself does not abolish the righting reflex inlaboratory animals such as mice when administered in up to lethal doses.

Thus the ability of the peptides of formula (I) and their salts and acidaddition salts both to induce and to maintain anaesthesia is not amorphine-like property.

As subclasses of the peptides of formula (I) and their salts and acidaddition salts may be mentioned those compounds wherein:

(i) R¹ is hydrogen;

(ii) m and n are both 0;

(iii) X³ is L-tyrosyl;

(iv) X⁴ is selected from D-methionyl, D-methionyl sulphoxide andD-methionyl sulphone, preferably from D-methionyl and D-methionylsulphoxide and is desirably D-methionyl sulphoxide;

(v) X⁶ is selected from L-phenylalanyl and L-4-nitrophenylalanyl and ispreferably L-4-nitrophenylalanyl;

(vi) X⁷ is selected from L-prolyl and D-prolyl and is preferablyL-prolyl;

(vii) p and q are both 0; and

(viii) R² is selected from --OR⁵ where R⁵ is preferably hydrogen, --NHR⁷where R⁷ is preferably selected from hydrogen and alkyl and is desirablyhydrogen, and --CH₂ OR⁸ where R⁸ is preferably hydrogen.

As a further subclass may be mentioned those peptides and their saltsand acid addition salts of the formula:

    H-Tyr-X.sup.4 -Gly-X.sup.6 --X.sup.7 --R.sup.2

wherein

X⁴ is selected from D-methionyl, D-methionyl sulphoxide and D-methionylsulphone;

X⁶ is selected from L-phenylalanyl, L-4-chlorophenylalanyl andL-4-nitrophenylalanyl;

X⁷ is selected from D-prolyl, L-prolyl, L-prolinol, D-leucyl,D-methionyl sulphoxide and cycloleucyl; and

R² is as defined in formula (I).

As a further subclass may be mentioned those peptides and their acidaddition salts of formula:

    H-Tyr-X.sup.4 -Gly-Phe (4NO.sub.2)-X.sup.7 -R.sup.2

wherein,

X⁴ is selected from D-methionyl sulphoxide and D-methionyl sulphone;

X⁷ is selected from L-prolyl, D-prolyl and L-prolinol; and

R² is selected from amino and monoalkylamino of one to four carbonatoms.

The peptides of formula (I) and their salts and acid addition salts maybe prepared by any of the methods known in the art for the preparationof compounds of analogous structure. Thus they may be formed by thesequential coupling of appropriate amino acids using either classicalmethods of peptide synthesis or solid phase procedures, or by theinitial preparation and subsequent coupling of peptide subunits.

Such reactions may be effected by, for example, activating thecarboxylic acid group of the ingoing amino acid and protecting thenon-reacting amino and carboxylic acid groups. Such techniques arestandard in the peptide art. Details of suitable activating andprotecting (masking) groups and of suitable reaction conditions (bothfor the coupling reactions and for the removal of protecting groups)giving the minimum of racemisation may be found in the followingliterature, all of which is incorporated herein by reference hereto,which is given purely by way of exemplification and which is intended tobe neither exhaustive nor limiting.

(a) Published United Kingdom patent specifications Nos. 1 042 487; 1 048086; and 1 281 383.

(b) Schroder and Luebke, "The Peptides" (Academic Press) (1965).

(c) Bellean and Malek, J. Am. Chem. Soc., 90, 165 (1968).

(d) Tilak, Tetrahedron Letters, 849 (1970).

(e) Beyerman, Helv. Chim. Acta., 56, 1729 (1973).

(f) Stewart and Young, "Solid Phase Peptide Synthesis" (W. H. Freemanand Co.) (1969).

Depending upon the reaction conditions the peptides of formula (I) areobtained in the form of the free base or as an acid addition salt orsalt thereof. The acid addition salts may be converted into the freebases or salts of other acids, and the bases may be converted into acidaddition salts thereof, by techniques well known in the art. Likewisethe peptides may be converted to salts thereof, and the salts convertedto the peptides or to other salts, by well established techniques.

The peptides of formula (I) and their salts and acid addition salts maythus be prepared by condensing a reagent (II)

    R.sup.1 -Y.sup.1 -OH                                       (II)

wherein Y¹ is selected from the radical (X¹)_(m) as defined in formula(I) and a partial radical sequence having the radical (X¹)_(m) at itsN-terminal end and from thereon corresponding to formula (I), with areagent (III)

    H-Y.sup.2                                                  (III)

wherein Y² corresponds to the balance of the above defined product, thereagents (II) and (III) being optionally protected and/or activatedwhere and as appropriate; followed if necessary and as appropriate byone or both of the steps of deprotection of the product and conversionof the product into the base or a salt or an acid addition salt thereof.

It will be appreciated by those skilled in the peptide art that thearginyl (D or L) and homoarginyl (Har) (D or L) radicals may not only beincorporated into the peptide chain in the fashion described above butmay also be formed in situ in the assembled chain, or in a subunitthereof, by guanidation of an ornithyl (D or L) or lysyl (D or L)radical respectively, using a reagent such as1-guanyl-3,5-dimethylpyrazole.

It will also be appreciated that other in situ conversions of thepeptides of formula (I) are possible. Thus the peptides wherein R² is agroup --NR⁶ R⁷ may be prepared by for example reaction of a peptidealkyl ester (wherein R² is --OR⁵ where R⁵ is alkyl) such as the methylester with ammonia, a heterocyclic base or a mono- or diamine, asappropriate. The peptide esters may be prepared from the peptide acids(R² is --OR⁵ where R⁵ is hydrogen) by standard esterification proceduresand the esters may be converted to the peptide acids by saponification.A hydroxy group Q¹ or Q² in respectively the radical X³ or X⁶ may beconverted to an alkoxy or benzyloxy group by the use of the appropriatediazoalkane, for example diazomethane to provide a methoxy group.Benzyloxy and alkanoyloxy identities for Q¹ and Q² may be converted tohydroxy groups by hydrogenolysis in methanol using 10% palladium oncharcoal catalyst and by alkaline hydrolysis respectively, and a hydroxygroup may be converted to an alkanoyloxy group by standard alkanoylationprocedures. All these are conventional techniques in the peptide art andreference may be made to the literature referred to hereinabove fordetails of reaction conditions and of appropriateprotection/deprotection procedures.

Because of their morphine agonist activity already alluded to thepeptides of formula (I) together with their pharmacologically andpharmaceutically acceptable salts and acid addition salts may be used inthe treatment of mammals in the fields of both human and veterinarymedicine in any condition where an agent with a morphine-like effect isindicated. Specific utilities that may be mentioned, by way of example,include the following:

(1) The relief of pain (analgesia), for example pain arising from spasmof smooth muscle as in renal or biliary colic, pain due to terminalillness such as cancer, pain in the post-operative period, andobstetrical pain.

(2) Sedation, for example in pre-anaesthetic medication;tranquillization; the induction of sleep, especially where sleeplessnessis due to pain or cough; and the relief of anxiety in general.

(3) The suppression of cough.

(4) The relief of dyspnoea, for example that of acute left ventricularfailure or pulmonary oedema.

(5) The induction of constipation, for example after ilcostomy orcolostomy, and the treatment of diarrhoea and dysentery.

(6) The induction of euphoria and the treatment of depression, forexample when allied to the relief of pain in terminal illness such ascancer.

The peptides of formula (I) and their pharmacologically andpharmaceutically acceptable salts and acid addition salts may also beused in the fields of both human and veterinary medicine for theinduction and/or maintenance of anaesthesia in a mammal.

A peptide or a salt thereof may be administered either alone as the soleanaesthetic agent or in combination with one or more other substanceswhich may complement and/or supplement its activity. Such additionalsubstances may be administered before, simultaneously with or afteradministration of the peptide or salt thereof and in the case ofsimultaneous administration the various agents may be administeredeither as separate doses or as a combination formulation.

As one possibility the peptide or salt thereof may be administeredsubsequent to administration of a benzodiazepine tranquillizer such aschlordiazepoxide (7-chloro-2-methylamino-5-phenyl-3H-1,4-benzodiazepine4-oxide),diazepam(7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one)andoxazepam(7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one).

As another possibility the peptide or salt thereof may be administeredfor the maintenance of anaesthesia after this has been initially inducedby the previous administration of another anaesthetic agent, for examplea barbiturate such as thiopental sodium (sodium5-ethyl-5-(1-methylbutyl)-2-thiobarbiturate).

A particular utility for the peptides of formula (I) and theirpharmacologically and pharmaceutically acceptable salts and acidaddition salts, within the field of anaesthesia, is the induction and/ormaintenance of the state referred to as "neuroleptanalgesia", acondition characterised by quiescence, psychic indifference toenvironmental stimuli, and analgesia (see, for example, Dorland'sIllustrated Medical Dictionary, twenty-fifth edition, published by W. B.Saunders, 1974, at page 1041, and "The Pharmacological Basis ofTherapeutics", Goodman, L.S. and Gilman, A. eds., fifth edition,published by Macmillan Publishing Co. Inc., 1975, especially at Chapter8, pages 97 to 101, all of which is incorporated herein by referencehereto). This condition is recognised by clinicians as desirable forenabling the performance of procedures such as bronchoscopy, X-raystudies, burn dressings and cystoscopy wherein a degree of patientcooperation is of value, and a fixed-dose combination comprising thenarcotic analgesic phentanyl citrate (N-(1-phenethyl-4-piperidyl)propionanilide citrate) and the neuroleptic agent droperidol(1-{1-[3-(p-fluorobenzoyl)propyl]-1,2,3,6-tetrahydro-4-pyridyl}-2-benzimidazolinone)has found acceptance for use in such circumstances.

In veterinary medicine two fixed-dose combinations comprising thenarcotic analgesic etorphine hydrochloride(4,5α-epoxy-3-hydroxy-6-methoxy-α,17-dimethyl-α-propyl-6,14-ethenomorphinan-7α(R)-methanolhydrochloride) together with either acepromazine(1-[10-[3-(dimethylamino)propyl]-10H-phenothiazin-2-yl]ethanone) ormethotrimeprazine(2-methoxy-N,N,β-trimethyl-10H-phenothiazine-10-propanamine) have foundacceptance for use in circumstances wherein a neuroleptanalgesic effectis required, for example in fracture reduction, wound stitching andcastration.

Heretofore neuroleptanalgesia has been achievable only uponadministration of such a drug combination as above mentioned. Thepeptides of formula (I) and their acceptable salts and acid additionsalts are thus an important clinical advance and valuable addition tothe armamentarium of the medical and veterinary professions in aloneenabling this result, without any additional medication being required.

For each of the utilities recited hereinbefore for the peptides offormula (I) and their salts and acid addition salts, that is to say,whether for use for the induction and/or maintenance of anaesthesia (forexample the induction and/or maintenance of neuroleptanalgesia) or foruse in a condition where an agent with a morphine-like effect isindicated (for example the utilities specifically identifiedhereinbefore under (1), (2), (3), (4), (5) or (6)) the amount requiredof the peptide or salt or acid addition salt thereof (hereafter referredto as the active ingredient) will vary with the route of administrationand with the nature and required extent of the desired effect, and willultimately be at the discretion of the physician or veterinarian. Ingeneral however for each of these utilities the dosage will be in therange 0.0025 μg to 40 mg per kilogram bodyweight of mammal, preferably0.025 μg to 10.0 mg/kg, more preferably 0.01 μg of 4.0 mg/kg andoptimally 0.25 to 400 μ g/kg (all dosages calculated with reference tothe peptide base). For use as an anti-diarrhoeal, an effective oral dosefor humans is a 3 mg. single dose given two or three times daily; foranti-tussive use an effective oral dose is 30 mg. single dose given twoor three times daily.

The active ingredients may be administered by any route appropriate tothe effect to be achieved, suitable routes including oral, rectal,nasal, topical (buccal), vaginal and parenteral (including subcutaneous,intramuscular and intravenous). It will be appreciated that thepreferred route will vary with the effect to be achieved and thus forexample in the relief of obstetrical pain administration directly intothe spinal cord may be advantageous.

While it is possible for the active ingredients to be administered asthe raw chemical it is preferable to present them as a pharmaceuticalformulation preparation.

The formulations, both veterinary and for human use, of the presentinvention comprise an active ingredient, as above defined, together withone or more acceptable carriers therefor and optionally othertherapeutic ingredients. The carrier(s) must be "acceptable" in thesense of being compatible with the other ingredients of the formulationand not deleterious to the recipient thereof. Desirably the formulationsshould not include oxidising agents and other substances with whichpeptides are known to be incompatible.

The formulations include those suitable for oral, rectal, nasal, topical(buccal), vaginal or parenteral (including subcutaneous, intramuscularand intravenous) administration, although the most suitable route in anygiven case will depend upon for example the active ingredient and thecondition to be treated. The formulations may conveniently be presentedin unit dosage form and may be prepared by any of the methods well knownin the art of pharmacy. All methods include the step of bringing intoassociation the active ingredient with the carrier which constitutes oneor more accessory ingredients. In general the formulations are preparedby uniformly and intimately bringing into association the activeingredient with liquid carriers or finely divided solid carriers orboth, and then, if necessary, shaping the product into the desiredformulation.

Formulations of the present invention suitable for oral administrationmay be presented as discrete units such as capsules, cachets or tabletseach containing a predetermined amount of the active ingredient; as apowder or granules; or as a solution or a suspension in an aqueousliquid or a nonaqueous liquid; or as an oil-in-water liquid emulsion ora water-in-oil liquid emulsion. The active ingredient may also bepresented as a bolus, electuary or paste.

A tablet may be made by compression or moulding, optionally with one ormore accessory ingredients. Compressed tablets may be prepared bycompressing in a suitable machine, the active ingredient in afree-flowing form such as a powder or granules, optionally mixed with abinder, lubricant, inert diluent, lubricating, surface active ordispersing agent. Moulded tablets may be made by moulding in a suitablemachine, a mixture of the powdered compound moistened with an inertliquid diluent.

Formulations for rectal administration may be presented as a suppositorywith the usual carriers such as cocoa butter, while a suitableformulation for nasal administration is nasal drops comprising theactive ingredient in aqueous or oily solution.

Formulations suitable for topical administration in the mouth includelozenges comprising the active ingredient in a flavoured basis, usuallysucrose and acacia or tragacanth; and pastilles comprising the activeingredient in an inert basis such as gelatin and glycerin, or sucroseand acacia.

Formulations suitable for vaginal administration may be presented aspessaries, creams, pastes or spray formulations containing in additionto the active ingredient such carriers as are known in the art to beappropriate.

Formulations suitable for parenteral administration convenientlycomprise sterile aqueous solutions of the active ingredient, whichsolutions are preferably isotonic with the blood of the recipient. Suchformulations may be conveniently prepared by dissolving solid activeingredient in water to produce an aqueous solution, and rendering saidsolution sterile and isotonic with the blood of the recipient. Theformulations may be presented in unit-or in multi dose containers, forexample scaled ampoules or vials.

Formulations suitable for nasal administration wherein the carrier is asolid include a coarse powder having a particle size for example in therange 20 to 500 microns which is administered in the manner in whichsnuff is taken, i.e. by rapid inhalation through the nasal passage froma container of the powder held close up to the nose.

It should be understood that in addition to the aforementionedingredients the formulations of this invention may include one or moreadditional ingredients such as diluents, buffers, flavouring agents,binders, surface active agents, thickeners, lubricants, preservatives(including anti-oxidants) and the like.

Where the formulation, for human or for veterinary use, is presented inunit dosage form, for example those unit dosage forms specificallymentioned above, each unit thereof conveniently contains the activeingredient (as above defined) in an amount in the range 0.125 μg. to 2g., preferably 1.25 μg. to 200 mg. and optionally 12.5 μg. to 20 mg.(all weights calculated with reference to the peptide base).

It will be appreciated from the foregoing that what we will claim maycomprise any novel feature described herein, principally and notexclusively, for example:

(a) The peptides of formula (I) as hereinabove defined together withtheir salts and acid addition salts.

(b) Methods as described hereinabove for the preparation of the peptidesof formula (I) and their salts and acid addition salts.

(c) Pharmaceutical formulations comprising a peptide of formula (I), apharmacologically and pharmaceutically acceptable salt thereof or apharmacologically and pharmaceutically acceptable acid addition saltthereof together with an acceptable carrier therefor.

(d) Methods for the preparation of the pharmaceutical formulationsdefined in (c) above.

(e) A method for the treatment of a mammal for a condition wherein anagent with a morphine-like effect is indicated, comprising theadministration to the mammal of a treatment effective non-toxic amountof a peptide of formula (I), a pharmacologically and pharmaceuticallyacceptable salt thereof or a pharmacologically and pharmaceuticallyacceptable acid addition salt thereof.

(f) A method according to (e) above for the treatment of a conditionselected from those specifically identified hereinabove under (1), (2),(3), (4), (5) or (6).

(g) A method for the induction and/or maintenance of anaesthesia in amammal, comprising the administration to the mammal of ananaesthetic-effective, non-toxic amount of a peptide of formula (I) or apharmacologically and pharmaceutically acceptable salt or acid additionsalt thereof.

(h) A method for the induction and/or maintenance of neuroleptanalgesiain a mammal, comprising the administration to the mammal of aneuroleptanalgesic-effective, non-toxic amount of a peptide of formula(I) or a pharmacologically and pharmaceutically acceptable salt or acidaddition salt thereof.

The following Examples serve to illustrate the present invention butshould not be construed as in any way providing a limitation thereof.All temperatures are in degrees Celsius.

Experimental Section

The following abbreviations are used throughout

HOBT--1-hydroxybenzotriazole

DCCI--dicyclohexylcarbodiimide

DCU--dicyclohexylurea

NMM--N-methylmorpholine

DMF--dimethylformamide

Pr--isopropanol

Pr₂ O--diisopropyl ether

pe--petroleum ether

EtOAc--ethyl acetate

Z--benzyloxycarbonyl

Bu--tertiary butyl

BOC--tertiary butyloxycarbonyl

Bzl--benzyl

Peptides were examined by tlc on Merck silica gel plates with thefollowing solvent systems:

1--Methylethylketone

2--n.Butanol:acetic acid:water (3:1:1)

3--Chloroform:methanol:32% acetic acid (120:90:40)

4--Chloroform:methanol:32% ammonia (120:90:40)

5--n.Butanol:acetic acid:ethylacetate:water (1:1:1:1)

6--Chloroform:methanol (8:1)

7--Chloroform:methanol:32% acetic acid (120:90:5)

8--Chloroform:methanol:32% ammonia (120:90:5)

Optical rotations were determined on a Bendix NPL automatic polarimeter.The amino acid compositions of peptide hydrolysates (6 N.HCl at 110° for24 hours in evacuated sealed tubes) were determined with aBeckman-Spinco Model 120C amino acid analyser or with a Rank Chromostakamino acid analyser.

The following general procedures were used throughout the syntheses ofthe peptides.

(a) Couplings were carried out in DMF and were mediated by DCCI.

(b) Amino acid ester hydrochlorides were converted to the free esters byaddition of a tertiary base, either triethylamine or N-methylmorpholine.

(c) HOBT was added at the coupling stage when segment condensationinvolved a peptide having an optically active carboxy terminal aminoacid.

(d) Couplings were allowed to proceed for 24 hours in the cold room at+4° C.

(e) After coupling, purification was effected by washing with acid andbase to remove unchanged reactants.

(f) Alkaline saponifications were carried out in aqueous methanol withan autotitrator at pH 11.5 to 12.0 with N.NaOH.

(g) Benzyloxycarbonyl protecting groups were removed by hydrogenolysisin methanol/acetic acid with 10% palladium on charcoal.

(h) The resulting acetate salts from the above hydrogenolysis wereconverted to the corresponding hydrochlorides by an addition ofmethanolic hydrogen chloride.

(i) Benzyl protecting groups were removed by hydrogenolysis in methanolwith 10% palladium on charcoal.

(j) Tertiary butyl and tertiary butyloxycarbonyl protecting groups wereremoved with N-hydrogen chloride in acetic acid, in the presence ofanisole to act as a scavenger. Cleavage was allowed to proceed for 60 to90 minutes.

(k) OBu protecting groups on the alcoholic functions of threonine andserine were removed with trifluoroacetic acid containing 10% water,cleavage being allowed to proceed for 90 minutes.

(l) The final peptides were isolated as their hydrochlorides and werelyophilised from aqueous solution.

EXAMPLE 1 H. Tyr. D-Met. Gly. Phe(4NO₂). Pro.NH₂

This was prepared according to the Scheme set out in Table 1. Theproduct was first isolated as the hydrochloride addition salt and thenpurified on carboxymethylcellulose (CMC 52) by gradient elution withammonium acetate buffers (0.001 M to 0.5 M). After lyophilisation fromaqueous solution the acetate addition salt had the followingcharacterising data:

Rf: 0.52² ; 0.83³ ; 0.47⁸.

[α]_(D) ²⁵ : +8.1° (C=0.2 in methanol).

EXAMPLE 2 H. Tyr. D-Met(O), Gly. Phe(4NO₂). Pro.NH₂

This was obtained from the acetate addition salt of Example 1 byoxidation with hydrogen peroxide in glacial acetic acid. The product, asthe acetate addition salt, had the following characterising data afterlyophilisation from aqueous solution:

Rf: 0.40² ; 0.68⁴.

[α]_(D) ²⁵ : +6.1° (C=0.12 in methanol).

The following peptides were prepared, with the characterising datarespectively shown therefor, according to standard procedures in peptidechemistry analogous to those set out in the foregoing Examples.C-Terminal derivatives are indicated according to convention, that is tosay:

--NH₂ : amide

--NHEt: ethylamide

--OMe: methyl ester

In the C-terminal residue (Pro.ol, i.e. prolinol) of the compounds ofExamples 7 and 9 the 1-carboxyl group of the conventional prolyl radicalis replaced by --CH₂ OH. In the preparation of these compounds the-Pro.ol group was introduced by reacting the appropriate complementaryreagent with H.Pro.ol, prepared by reduction of proline methyl ester (H.Pro. OMe) with sodium borohydride. The final intermediate was in eachcase the corresponding BOC-tyrosyl pentapeptide which was deprotected byreaction with trifluoroacetic acid in the presence of anisole.

The following procedure illustrates the preparation of analogues ofphenylalanine substituted in the para position by the sulphur containingresidues CH₃.S--; CH₃.SO-- and CH₃.SO₂ --. ##STR6## which are present inthe peptides of Examples 17, 18 and 19:

The DL amino acids were prepared by the method of Colescott et al.J.A.C.S. 79, 4232 (1957) (copy attached). The routes are outlined belowand the number given to each compound corresponds to that used in theabove paper. ##STR7##

Each of the DL amino acids was acetylated and resolved by the use of hogrenal acylase to give the L-amino acid and the D-acetyl amino acid.[Biochim. Biophys.Acta 148, 414 (1967). Helv.Chim.Acta 59, 2181 (1976).]##STR8## The following illustrates the enzymic resolution ofN-acetyl-p-methyl sulphinyl-DL-phenylalanine:

The acetyl-DL-amino acid (6.75 g, 25 millimoles) was dissolved in 150mls of water and the pH was adjusted to 7.5 by the addition of Nammonium hydroxide solution. Acylase (50 mg) and cobalt acetate (200 mg)were added and the mixture was stirred gently at 38° C. overnight.

The pH was adjusted to 5.5 by the addition of acetic acid and thesolution was passed through a 4×30 cm column of Dowex AG 50×2 resin.After the column had been washed with water the L-amino acid was elutedwith 0.5 m ammonia.

The L-amino acids were converted to their t-butyloxycarbonyl derivativesand incorporated into the peptide chain by the normal methods of peptidechemistry. The general method is shown in the Scheme below. The variouscoupling stages may either be mediated by DCCl/HOBT or carried out bythe mixed anhydride procedure ##STR9## The following illustrates thepreparation of analogues containing L-(-)-pipecolinic acid(L-(-)-hexahydropyridine-2-carboxylic acid):

The synthesis of the peptide of Example 12 requires as an intermediatethe amide of L-(-)-pipecolinic acid. This was obtained according to theScheme below: ##STR10##

The synthesis of the peptide of Example 12 then proceeds in similarmanner to the Scheme already provided and involves the fragmentcondensation of: ##STR11##

The penultimate peptide is therefore; ##STR12## from which theprotecting group is removed by N-hydrogen chloride in glacial aceticacid in the presence of anisole as a scavenger.

The following illustrates the preparation of analogues containingβ-homoproline (pyrrolidine-2-acetic acid):

BOC L-proline is homologated as described by M. A. Ondetti and S. L.Engel (J.Med.Chem., 18, 761 (1975)).

BOC.L-homoPro is then converted via the mixed anhydride procedureoutlined above to BOC.L-homoPro.NH₂ from which L-homoPro.NH₂.HCl isobtained by deprotection with N.HCl/HOAc.

The peptide of Example 21 is prepared in the normal manner from thefragements: ##STR13##

The Met residue in position 2 may then be converted to the sulphoxide bytreatment with H₂ O₂. ##STR14##

                                      TABLE 1                                     __________________________________________________________________________    Ex. No.                                                                              Compound                  Rf    [α].sub.D.sup.25 (in                                                    methanol)                              __________________________________________________________________________    3.   H.Try.D-Met.Gly.Phe.D-Pro.OH HCl                                                                        0.51.sup.7 ;0.48.sup.8                                                                +48.3° (c = 0.2)                4.   H.Tyr.D-Met.Gly.Phe(4NO.sub.2).Pro.OH HCl                                                               0.44.sup.2 ;0.46.sup.8                                                                -2.8° (c = 0.2)                 5.   H.Tyr.D-Met.Gly.Phe(4NO.sub.2).Pro.ol                                                                   0.56.sup.2 ;0.75.sup.7 ;0.71.sup.8                                                    +22.9° (c = 0.2)                     trifluoroacetate                                                         6.   H.Tyr.D-Met(O).Gly.Phe(4NO.sub.2).Pro.ol                                      trifluoroacetate          0.40.sup.8                                                                            +12.9° (c = 0.22)               7.   H.Tyr.D-Met(O.sub.2).Gly.Phe(4NO.sub.2).Pro.NH.sub.2                                                    0.32.sup.2 ;0.65.sup.3 ;0.64.sup.4                                                    +6.3 (c = 0.2)                         8.   H.Tyr.D-Met.Gly.Phe.D-Leu 0.61.sup.2 ;0.54.sup.7 ;0.43.sup.8                                                    +7.1° (c = 0.2)                 9.   H.Tyr.D-Met.Gly.Phe(4Cl).Pro.NH.sub.2                                                                   0.49.sup.2 ;0.92.sup.3 ;0.82.sup.4                                                    +10.0 (c = 0.2)                        10.  Tyr.D-Met(O).Gly.Phe(4Cl).Pro.NH.sub.2                                                                  0.60.sup.4                                                                            +11.6° (c = 0.1)                11.  Tyr.D-Met(O).Gly.Phe.D-Leu                                                                              0.40.sup.2 ;0.40.sup.7 ;0.15.sup.8                                                    +34.2° (c = 0.2)                12.  Tyr.D-Met.Gly.Phe(4NO.sub.2).Pec.NH.sub.2.HCl                                                           0.52.sup.2 ;0.93.sup.3                                                                +7.3° (c = 0.2)                 13.  Tyr.D-Met.Gly.Phe(4NO.sub.2).D-Met.NH.sub.2.HOOCCH.sub.3                                                0.53.sup.2 ;0.56.sup.7                                                                +35.4°  (c = 0.2)               14.  Tyr.D-Met.Gly.Phe(4NO.sub.2).D-Pro.NH.sub.2.HCl                                                         0.49.sup.2 ;0.55.sup.7 ;0.54.sup.8                                                    +45.3° (c = 0.2)                15.  Tyr.D-Met(O).Gly.Phe(4NO.sub.2).D-Pro.NH.sub.2.HOOCCH.sub.3                                             0.52.sup.7                                                                            +17.3° (c = 0.2)                16.  Tyr.D-Met(O).Gly.Phe(4CF.sub.3).Pro.NH.sub.2.HCl                                                        0.39.sup.2 ;0.50.sup.7 ;0.63.sup.8                                                    +6.43° (c = 0.4)                17.  Try.D-Met.Gly.Phe(4SO.sub.2 Me).Pro.NH.sub.2.HOOCCH.sub.3                                               0.30.sup.2 ;0.57.sup.7 ;0.24.sup.8                                                    --                                     18.  Tyr.D-Met.Gly.Phe(4SOMe).Pro.NH.sub.2.HOOCCH.sub.3                                                      0.27.sup.2 ;0.58.sup.7 ;0.34.sup.8                                                    --                                     19.  Tyr.D-Met.Gly.Phe(4SMe).Pro.NH.sub.2.HOOCCH.sub.3                                                       0.27.sup.2 ;0.55.sup.7 ;0.75.sup.8                                                    +17.8° (c = 1.0)                20.  Tyr.D-Met.Gly.Phe(4CF.sub.3).Pro.NH.sub.2 HCl                                                           0.48.sup.2 ;0.45.sup.7 ;0.42.sup.8                                                    +4.1° (c = 0.4)                 21.  Tyr.D-Met.Gly.Phe(4NO.sub.2).homoPro.NH.sub.2                                                           0.52.sup.2 ;0.15.sup.5                                                                +12.9° (c                       __________________________________________________________________________                                           = 0.2)                             

EXAMPLE 22 Pharmacological Activity

Peptides of the foregoing Examples were tested for the followingactivities according to standard pharmacological procedures.

(A) Analgesia in mice in the hot plate test (modification of the methodof Eddy, N. B. et al., J. Pharm. Exp. Therap. (1953) 107, 385, thepeptide being administered by intracerebroventricular injection).

(B) Antidiarrhoeal activity in the rat. In this procedure rats werestarved for 24 hours, the peptide then administered either sucutaneouslyor orally followed after 15 minutes by 1 ml. castor oil per rat givenorally.

(C) For anti-tussive testing, guinea-pigs were subjected to an aerosolcontaining 20% citric acid, 30 minutes after administration of compound(orally or subcutaneously). The number of coughs during a five minuteexposure are counted and meaned for six animals per treatment. Themethod is that described by Boura, A. L. A., Green, A. F. and Saunders,I. A. Br. J. Pharmac., May 1970, Vol. 39, No. 1, page 225.

(D) Analgesia in mice in the writhing test (modification of the methodof Henderson et al. (J. Pharm. Exp. Therap., 125, (1959), 237) thepeptide being administered orally.

From the data obtained the respective ED₅₀ figures were calculated (i.e.the dose required to elicit the appropriate effect in 50% of theanimals). N.T.: not tested.

    __________________________________________________________________________           RESULTS EXPRESSED AS ED.sub.50 :                                              ANALGESIA:-                                                                   MOUSE HOT                   ANALGESIA:-                                       PLATE   ANTIDIARRHOEA                                                                            ANTITUSSIVE                                                                            WRITHING                                   Peptide of                                                                           μg/mouse                                                                           mg/kg (rat)                                                                              mg/kg    mg/kg                                      Example No.                                                                          i.c.v.  s.c.  p.o. (guinea-pig)                                                                           (mouse)                                    __________________________________________________________________________    1      0.007   0.05  2    0.7 p.o. 35 p.o.                                    2      0.005   0.02  0.05 0.7 p.o. 2 p.o.                                                               0.02 s.c.                                           3      0.005   2     7    None at  NT                                                                   10 p.o.                                             4      0.07    0.2   None at                                                                            NT       NT                                                              10                                                       5      0.05    0.03  0.3  >10 p.o. NT                                         6      0.0007  0.05  0.2  9 p.o.   NT                                         7      0.00008 0.05  0.3  3 p.o.   NT                                         8      0.07    5     >10  NT       NT                                         9      0.005   0.2   10   NT       NT                                         10     0.0008  0.02  1    >10 p.o. NT                                         11     0.001   0.7   >10  NT       NT                                         12     0.008   0.3   8    NT       NT                                         13     0.005   1     >10  >10 p.o. NT                                         14     0.003   0.02  0.2  <10 p.o. NT                                         15     0.003   0.02  0.1  10 p.o.  3 p.o.                                     16     0.003   0.03  2    None at 3 p.o.                                                                         NT                                         17     0.08    None at                                                                             None at                                                                            NT       NT                                                        1     10                                                       18     0.03    None at                                                                             None at                                                                            NT       NT                                                        1     10                                                       19     0.8     8     None at                                                                            NT       NT                                                              10                                                       20     0.07    0.1   8    NT       NT                                         21     0.003   0.03  2    NT       NT                                         __________________________________________________________________________

EXAMPLE 23 Pharmaceutical Formulations (A) Tablet Formulation (20mg/tablet)

Compound of formula (I): 20 mg

Lactose: 76 mg

Maize Starch: 10 mg

Gelatin: 2 mg

Magnesium Stearate: 2 mg

Mix together the compound of formula (I), Lactose and Maize Starch.Granulate with a solution of the Gelatin dissolved in water. Dry thegranules, add the Magnesium Stearate and compress to produce tablets,110 mg per tablet.

(B) Suppository (5 mg/product)

Compound of formula (I): 250 mg

Suppository Base (Massa Esterinum C): to 100 g

Melt the suppository base at 40° C. Gradually incorporate the compoundof formula (I) in fine powder form and mix until homogeneous. Pour intosuitable moulds, 2 g per mould, and allow to set.

Massa Esterinum C is a commercially available suppository baseconsisting of a mixture of mono, di, and triglycerides of saturatedvegetable fatty acids. It is marketed by Henkel International,Dusseldorf.

(C) Pessary (5 mg/product)

Compound of formula (I): 5 mg

Lactose: 400 mg

Povidone: 5 mg

Magnesium Stearate: 5 mg

Mix together the compound of formula (I) and Lactose. Granulate with asolution of Povidone in 50% aqueous ethanol. Dry the granules add themagnesium Stearate and compress on suitably shaped punches, 415 mg perpessary.

(D) Freeze-dried Injection 100 mg/vial

Compound of formula (I): 100 mg

Water for Injections to: 2.0 ml

Dissolve the compound of formula (I) in the Water for Injections.Sterilise the solution by passage through a membrane filter, 0.2 μm poresize, collecting the filtrate in a sterile receiver. fill into sterileglass vials, 2 ml/vial under aseptic conditions and freeze-dry. Closethe vials with sterile rubber closures secured with an aluminium seal.

The injection is reconstituted prior to administration by the additionof a convenient volume of Water for

Injections or sterile saline solution.

In the foregoing, the weight of the compound of formula (I) is in eachinstance calculated with reference to the peptide base.

What we claim is:
 1. Tyr.D-Met. Gly. Phe(4NO₂). ProNH₂.
 2. Apharmaceutically acceptable acid addition said of Tyr.D-Met.Gly.Phe(4NO₂). ProNH₂.
 3. The acetate salt of claim
 2. 4. Apharmaceutical composition for use as an antidiarrhoeal comprising aneffective antidiarrhoeal amount of H.Tyr.D-Met.Gly.Phe(4NO₂).Pro.NH₂ ora pharmaceutically acceptable acid addition salt thereof together with apharmaceutically acceptable liquid or solid carrier therefor.
 5. Thecomposition of claim 4 in a form suitable for oral, rectal or parenteraladministration.
 6. The composition of claim 5 in the form of a tablet.7. The composition of claim 5 in the form of a capsule.